FDA Import Refusal AEK-9366612-9/10003/1 — EMBRAMED MATRIZ CREMER SA
The FDA refused shipment AEK-9366612-9/10003/1 from EMBRAMED MATRIZ CREMER SA (Brazil) on Feb 27, 2026. The refused product falls under Devices — CATHETER, RETENTION TYPE, BALLOON. Cited charges: 118,3280,341
Refusal Details
- Date
- Feb 27, 2026
- Country
- Brazil
- Product Category
- Devices
- Product Code
- 78EZL CATHETER, RETENTION TYPE, BALLOON
- Charges
- 118,3280,341